TY - JOUR
T1 - Feline Morbillivirus
T2 - Clinical Relevance of a Widespread Endemic Viral Infection of Cats
AU - Pennisi, Maria Grazia
AU - Belák, Sándor
AU - Tasker, Séverine
AU - Addie, Diane D
AU - Boucraut-Baralon, Corine
AU - Egberink, Herman
AU - Frymus, Tadeusz
AU - Hartmann, Katrin
AU - Hofmann-Lehmann, Regina
AU - Lloret, Albert
AU - Marsilio, Fulvio
AU - Thiry, Etienne
AU - Truyen, Uwe
AU - Möstl, Karin
AU - Hosie, Margaret J
PY - 2023/10/13
Y1 - 2023/10/13
N2 - Feline morbillivirus (FeMV) was first isolated in 2012 from stray cats in Hong Kong. It has been found in association with tubulointerstitial nephritis (TIN), the most common cause of feline chronic kidney disease (CKD). However, viral host spectrum and virus tropism go beyond the domestic cat and kidney tissues. The viral genetic diversity of FeMV is extensive, but it is not known if this is clinically relevant. Urine and kidney tissues have been widely tested in attempts to confirm associations between FeMV infection and renal disease, but samples from both healthy and sick cats can test positive and some cross-sectional studies have not found associations between FeMV infection and CKD. There is also evidence for acute kidney injury following infection with FeMV. The results of prevalence studies differ greatly depending on the population tested and methodologies used for detection, but worldwide distribution of FeMV has been shown. Experimental studies have confirmed previous field observations that higher viral loads are present in the urine compared to other tissues, and renal TIN lesions associated with FeMV antigen have been demonstrated, alongside virus lymphotropism and viraemia-associated lymphopenia. Longitudinal field studies have revealed persistent viral shedding in urine, although infection can be cleared spontaneously.
AB - Feline morbillivirus (FeMV) was first isolated in 2012 from stray cats in Hong Kong. It has been found in association with tubulointerstitial nephritis (TIN), the most common cause of feline chronic kidney disease (CKD). However, viral host spectrum and virus tropism go beyond the domestic cat and kidney tissues. The viral genetic diversity of FeMV is extensive, but it is not known if this is clinically relevant. Urine and kidney tissues have been widely tested in attempts to confirm associations between FeMV infection and renal disease, but samples from both healthy and sick cats can test positive and some cross-sectional studies have not found associations between FeMV infection and CKD. There is also evidence for acute kidney injury following infection with FeMV. The results of prevalence studies differ greatly depending on the population tested and methodologies used for detection, but worldwide distribution of FeMV has been shown. Experimental studies have confirmed previous field observations that higher viral loads are present in the urine compared to other tissues, and renal TIN lesions associated with FeMV antigen have been demonstrated, alongside virus lymphotropism and viraemia-associated lymphopenia. Longitudinal field studies have revealed persistent viral shedding in urine, although infection can be cleared spontaneously.
KW - Cats
KW - Animals
KW - Clinical Relevance
KW - Cross-Sectional Studies
KW - Morbillivirus/genetics
KW - Morbillivirus Infections/epidemiology
KW - Renal Insufficiency, Chronic/veterinary
KW - Nephritis, Interstitial/epidemiology
KW - Cat Diseases/epidemiology
U2 - 10.3390/v15102087
DO - 10.3390/v15102087
M3 - Review article
C2 - 37896864
SN - 1999-4915
VL - 15
JO - Viruses
JF - Viruses
IS - 10
M1 - 2087
ER -